Extended labeling issued for Euflexxa

Article

Changes to the labeling for Euflexxa (1% sodium hyaluronate, Ferring Pharmaceuticals), a treatment for the pain associated with osteoarthritis, have been approved by the FDA.

Changes to the labeling for Euflexxa (1% sodium hyaluronate, Ferring Pharmaceuticals), a treatment for the pain associated with osteoarthritis, have been approved by the FDA. The product can now be stored at room temperature, as well as refrigerated. The new labeling will make it easier for physicians to store the drug and keep it available for patients, according to the company. The highly purified hyaluronan product is a non-avian-derived hyaluronic acid that is administered as a three-injection treatment regimen for patients who have failed to adequately respond to conservative nonpharmacologic therapy and simple analgesics.

To see more Hot off the Press news articles, click here http://www.drugtopics.com/Hot+off+the+Press.

To go to the Drug Topics homepage, click here http://www.drugtopics.com.

Newsletter

Pharmacy practice is always changing. Stay ahead of the curve with the Drug Topics newsletter and get the latest drug information, industry trends, and patient care tips.

Recent Videos
2 experts are featured in this series.
2 experts are featured in this series.
2 experts are featured in this series.
2 experts are featured in this series
Image Credit: jokekung - stock.adobe.com
Related Content
© 2025 MJH Life Sciences

All rights reserved.